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NCT00517348 · ClinicalTrials.gov registry record · Phase 1

Study Evaluating IMA-026 in Healthy Subjects

A Phase 1 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

Completed
Registry status
Phase 1
Development phase
50
Enrollment target

NCT00517348: Completed Phase 1 study, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

NCT00517348 is a Phase 1 study that has completed, run by Wyeth is now a wholly owned subsidiary of Pfizer. The registered enrollment target is 50 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (17% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT00517348, a Phase 1 study, has completed, sponsored by Wyeth is now a wholly owned subsidiary of Pfizer.

COMPLETED
Registry status
Phase 1
Development phase
50 participants
Enrollment target

Study Summary

To assess the safety, tolerability, pharmacokinetics, and pharmacodynamics of IMA-026 administered subcutaneously (SC) or intravenously (IV) in healthy adults.

Interventions

  • BIOLOGICAL IMA-026

Trial Details

FieldValue
Enrollment Target 50 participants
Start Date 2007-09
Est. Completion 2008-07
Phase Phase 1

What the finished NCT00517348 record still lists

NCT00517348 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 50 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (17% lower).

The record links to 0 conditions, and to 1 intervention - of which IMA-026 is the first listed.

NCT00517348 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT00517348 about?

NCT00517348 is a clinical study titled "Study Evaluating IMA-026 in Healthy Subjects". To assess the safety, tolerability, pharmacokinetics, and pharmacodynamics of IMA-026 administered subcutaneously (SC) or intravenously (IV) in healthy adults.

What is the current status of trial NCT00517348?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 50 participants. The study started on 2007-09. Estimated completion is 2008-07.

What interventions are being tested in trial NCT00517348?

The interventions under investigation include: IMA-026 (BIOLOGICAL).

Who is sponsoring clinical trial NCT00517348?

This trial is sponsored by Wyeth is now a wholly owned subsidiary of Pfizer, which has 167 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT00517348's enrollment target sits among peer trials

50 973rd of 2000 higher than 984 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT00517348, the US trial registry maintained by the National Library of Medicine. NCT00517348 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.